EP2102376B1 - Annealing and pickling process - Google Patents

Annealing and pickling process Download PDF

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Publication number
EP2102376B1
EP2102376B1 EP07847161A EP07847161A EP2102376B1 EP 2102376 B1 EP2102376 B1 EP 2102376B1 EP 07847161 A EP07847161 A EP 07847161A EP 07847161 A EP07847161 A EP 07847161A EP 2102376 B1 EP2102376 B1 EP 2102376B1
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comprised
heating
strip
temperature
atmosphere
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German (de)
English (en)
French (fr)
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EP2102376A1 (en
Inventor
Alessandro Dulcetti
Milorad Pavlicevic
Nicoletta Zacchetti
Alessandra Primavera
Stefano Luperi
Luca Lattanzi
Simone Guanin
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Danieli and C Officine Meccaniche SpA
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Danieli and C Officine Meccaniche SpA
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    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D9/00Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
    • C21D9/52Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for wires; for strips ; for rods of unlimited length
    • C21D9/54Furnaces for treating strips or wire
    • C21D9/56Continuous furnaces for strip or wire
    • C21D9/561Continuous furnaces for strip or wire with a controlled atmosphere or vacuum
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25FPROCESSES FOR THE ELECTROLYTIC REMOVAL OF MATERIALS FROM OBJECTS; APPARATUS THEREFOR
    • C25F1/00Electrolytic cleaning, degreasing, pickling or descaling
    • C25F1/02Pickling; Descaling
    • C25F1/04Pickling; Descaling in solution
    • C25F1/06Iron or steel
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D9/00Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
    • C21D9/52Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for wires; for strips ; for rods of unlimited length
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D9/00Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
    • C21D9/52Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for wires; for strips ; for rods of unlimited length
    • C21D9/54Furnaces for treating strips or wire
    • C21D9/56Continuous furnaces for strip or wire
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23GCLEANING OR DE-GREASING OF METALLIC MATERIAL BY CHEMICAL METHODS OTHER THAN ELECTROLYSIS
    • C23G1/00Cleaning or pickling metallic material with solutions or molten salts
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23GCLEANING OR DE-GREASING OF METALLIC MATERIAL BY CHEMICAL METHODS OTHER THAN ELECTROLYSIS
    • C23G1/00Cleaning or pickling metallic material with solutions or molten salts
    • C23G1/02Cleaning or pickling metallic material with solutions or molten salts with acid solutions
    • C23G1/08Iron or steel
    • C23G1/085Iron or steel solutions containing HNO3
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23GCLEANING OR DE-GREASING OF METALLIC MATERIAL BY CHEMICAL METHODS OTHER THAN ELECTROLYSIS
    • C23G1/00Cleaning or pickling metallic material with solutions or molten salts
    • C23G1/02Cleaning or pickling metallic material with solutions or molten salts with acid solutions
    • C23G1/08Iron or steel
    • C23G1/086Iron or steel solutions containing HF

Definitions

  • the present invention relates to a continuous annealing and pickling process of flat rolled products, specifically to an annealing and pickling process of cold-rolled stainless steel strips.
  • the production cycle of flat rolled stainless steel sections contemplates various mechanical treatment steps, such as rolling, thermal treatment steps, such as annealing, and surface treatment steps, such as descaling, pickling, passivation and finishing.
  • a stainless steel strip is firstly annealed to allow the solubilization of chromium carbides and the re-crystallisation of the material, then pickled to remove scale from the surface and finally cold-rolled to reach the final required thickness.
  • the annealing and pickling treatments of hot-rolled sections are usually performed on continuous annealing and pickling lines, sometimes capable of also processing cold-rolled sections.
  • the cold-rolling treatment of strips generally contemplates final thickness reductions from 20% to 85% by means of a sequence of rolling steps.
  • the final roughness of the surface of the cold-rolled sections is comprised from 0,01 to 0,50 ⁇ m.
  • the stainless steel strip is then subjected to a further thermal treatment cycle, during which there are provided the processes of re-crystallisation and grain growth, which is aimed at conferring to the final product the required mechanical features, e.g. those contemplated by standard EN 10088.
  • a cooling section for cooling the strip, from the maximum temperature reached in the furnace down to temperatures lower than 80°C, is always present downstream of the section of said further thermal treatment, on both CA&P lines and on BA lines.
  • air or preferably O 2 content controlled atmosphere jet-coolers are normally used up to temperatures of the strip of approximately 750-650°C.
  • the strip is cooled with jet-coolers in H 2 /N 2 atmosphere up to the final temperature lower than approximately 100°C.
  • the cooling rate is higher than 15-20°C/s to avoid phenomena of chromium carbide precipitation at the grain boundaries which make the steel sensitive to the so-called intergranular corrosion.
  • the introduction of cooling gas is dimensioned and adjusted to also ensure the required planarity of the strips, specifically the thin ones.
  • the strip and its support during all steps of the treatment are typically conveyed by means of conveying systems, generally roller systems, which come into contact with the surface of the strip.
  • conveying systems generally roller systems
  • the contact of the strip, at high temperatures, with the surface of said systems is avoided in order to prevent surface defects.
  • the safety constraints deriving from the use of atmospheres containing high quantities of H 2 , for which the possibility of contact with air must be prevented determine the convenience of excluding any strip conveying system of the roller type within the heating furnace, imposing in fact the use of exclusively vertical closed annealing furnaces for this type of process.
  • the BA lines typically consist of vertically developed heating and cooling sections, in which the strip undergoes the heating and cooling treatments moving always in vertical direction, without the need for conveying systems and/or support in contact with the strip when this is at high temperatures.
  • the intrinsic mechanical features of the flat rolled stainless steel sections, e.g. the tensile yield stress, and of the metallic structures of the furnaces themselves limit the maximum reachable height of the BA lines and consequently the maximum reachable production rate, which is thus generally no higher than 20 tons/h, considerably lower than that of CA&PLs, which is generally comprised from 50 to 150 tons/h.
  • Bright Annealing lines thus allow to obtain a strip surface with final finish having a higher reflectivity with respect to CA&PLs but display, with respect to the latter, a lower production rate and higher costs.
  • the annealing thermal treatment performed in oxidising atmosphere (CA&PLs), causes the formation, on the strip surface, of a layer of oxides and a layer of dechromized steel underneath, i. e. chromium-depleted steel. Both layers are then removed in appropriate manner to impart the required final surface features to the material.
  • the thermal treatment is thus followed by a further sequence of chemical and electrochemical treatments of descaling, pickling and passivation, which aim at obtaining a finished product characterised by an oxide-free surface and, in general principle, dull, hence the name "2D" (according to the Standard EN 10088) wherein D stands for "dull".
  • the pickling systems for cold-rolled product processing lines normally consist of a descaling section, a pickling section and a passivation section.
  • the scale formed during the annealing process is conditioned and partially removed facilitating the intervention of the downstream removal processes.
  • the cold-rolled strip descaling technologies normally used are either of the thermochemical type, using oxidising dissolved salt baths, e.g. kolene (eutectic mixture of NaOH, NaNO 3 NaCl), or of the electrolytic type, using both neutral sodium sulphate solutions and acid solutions. Both the chemical technologies in dissolved salt baths and the electrolytic technologies perform a selective oxidation of the chromium present in the oxide making it soluble in the bath.
  • a method for obtaining electrochemically said descaling treatment is described in WO02/086199 in which the density of applied current and the specific electric charge transferred to the strip are correlated to the features of the oxide to be removed.
  • the dechromized steel layer, formed during annealing, is removed and the removal of the oxide layer, anchored to it, is completed by means of the action of acid baths having a high oxidising capacity and formed by mixtures of mineral acids.
  • acid baths having a high oxidising capacity and formed by mixtures of mineral acids.
  • the most commonly used baths are mixtures of mineral acids, such as: HNO 3 -HF at temperatures from 25 to 70°C, and mixtures of H 2 SO 4 -HF, with the addition of oxidising agents and operated at temperatures from 25 to 70°C, as for example described in EP1490531 .
  • the final passivation treatment leads to the formation, on the surface of the finished product, of the necessary protective passivation film. Said action is generally obtained by means of high redox potential baths, when not performed at the same time as the pickling action.
  • the behaviour of the material surface to the descaling, pickling and finishing/passivation treatment depends on the features of the oxide layer and on entity of the layer of dechromized steel underneath. Such features are affected by the type of material, the chemical composition of the steel (content of Cr, Ni, Mn, Si, etc.), the thermal cycle undergone by the strip (in terms of maximum reached temperature, permanence time over a determined temperature, heating and cooling rates) and the chemical composition of the atmosphere in the furnace (concentration of oxidising agents O 2 , H 2 O and CO 2 ).
  • US4713154 describes a process and the related apparatus in which, in order to reduce the thickness of the oxide layer and favour its pickling potential, the strip is annealed in sealed furnaces, horizontally or vertically developed, in which the atmosphere is formed by nitrogen and hydrogen with concentration of the latter comprised from 3 to 15%.
  • the strip remains for a time such that the entire annealing and cooling cycle is carried out in atmosphere of N 2 -H 2 , said strip following internal horizontal and/or vertical paths, being guided by a complex support roller system.
  • the subsequent pickling occurs in electrolytic cells containing nitric acid.
  • JP5222449 describes a process for controlling the structure and the thickness of the oxide film which is generated during the annealing process for improving the pickling properties and the surface quality of the cold-rolled Fe-Cr or Fe-Cr-Ni stainless steels.
  • the combustion gas atmosphere is controlled, specifically the content of O 2 is set to values of ⁇ 1 % when the strip temperature is ⁇ 600 °C for Fe-Cr steels and ⁇ 800°C for Fe-Cr-Ni steels, while over 600°C for Fe-Cr steels and 800°C for Fe-Cr-Ni steels the O 2 concentration is set to values comprised from 1% to 10% up to the maximum annealing temperature.
  • the heating rate of the strips of equal thickness depends on the zone temperature in that segment of the furnace. Considering that usually the furnace zone temperatures do not exceed 1200-1250°C and considering the emissivity values of stainless steel strips, comprised from 0,25 to 0,45 according to the input surface state, the temperature, the type of steel, etc., the average thermal flow received by the strip is generally comprised from 10 to 65 kW/m 2 for each face of the strip and generally does not exceed 70 kW/m 2 . Consequently, the heating rate of 1 mm thick strips is generally comprised from 25 to 35°C/s and does not exceed 40°C/s.
  • the atmosphere in the CA&PL burner furnaces is essentially regulated/controlled by acting on the supporter of combustion/fuel ratio ( ⁇ ) in the burners and appears formed by different oxidising species: carbon dioxide, aqueous vapour and quantities of oxygen in excess with respect to stoichiometric combustion ⁇ >1.
  • the ratio ⁇ is set to obtain an excess of O 2 equal to 2-5% for austenitic stainless steels and equal to 4-10% for ferritic stainless steels.
  • a 1 mm thick strip of AISI 304 annealed with a standard thermal cycle which allows to obtain the required mechanical properties (ref. EN10088), with maximum temperature of 1110°C and permanence time of 60 seconds, and with an O 2 content in atmosphere of 3-5%, is characterised by an oxide layer generally comprised from 300 to 400 nm, formed by mixed chromium, iron, manganese and silicon oxide. Specifically, starting from the interface with the matrix, the oxide is characterised by a first slightly Si enriched layer, by a subsequent Cr enriched layer and by an external mixed Cr and Fe layer enriched with Mn.
  • said dissolution leads to the formation of high environmental impact chemical reaction products both in gaseous phase, such as fumes or acid bath vapours, and in liquid phase, such as exhausted treatment solutions and wash water.
  • the hourly quantities of said reaction products are directly proportional to the specified quantity, per area unit, of removed oxide and dechromized steel. It is thus required to make a further treatment section, auxiliary to the descaling, pickling and finishing/passivation sections, dedicated to the neutralisation/laying of the aforesaid chemical reaction products, with increased times and production costs.
  • the present invention thus aims to solve the above discussed problems by making a continuous annealing and pickling process for flat cold-rolled stainless steel products of thickness comprised from 0,3 to 4 mm, having surface roughness Ra ⁇ 0,50 ⁇ m, which, comprises the steps of the claim 1.
  • the inert agents are formed by N 2 and the reducing agents are formed by H 2 .
  • the process of the present invention allows to obtain products of higher surface quality with respect to that obtainable with the conventional annealing and pickling lines (CA&PL) and tending to the surface quality obtained with Bright Annealing (BA) lines.
  • the obtained surface reflectivity measured as percentage of the light reflected at an angle of 60° with respect to the vertical of the surface, tends to be that of the material obtained by a BA process, for example higher than 50% for AlSI 304 type austenitic steels.
  • the present invention also allows to obtain a further significant advantage in terms of cost reduction for the production of high surface quality strips. Indeed, such process has a productivity similar with respect to that of the conventional continuous treatment lines and thus considerably higher with respect to that obtainable in BA lines due to the known constraints related to vertical development.
  • the process described in the present invention determines the formation, during the annealing step, of a layer of oxide which displays:
  • the reduction of the environmental impact advantageously derives from the lower consumption of acids per area unit of processed strip. This occurs by effect of the reduction of the amount of steel to be dissolved during the pickling step, being the layer of oxide and of dechromized steel to be removed smaller with respect to that produced during the conventional annealing procedures.
  • the stainless steels treatable with the process of the invention are all those produced in the form of cold-rolled sections, including, for example:
  • the process object of the present invention is applied to a product, stainless steel cold-rolled strip of thickness comprised from 0,3 to 4 mm, having the following surface features: roughness Ra ⁇ 0,50 ⁇ m and preferably Ra ⁇ 0,10 ⁇ m and possibly degreased.
  • the continuous annealing and pickling process of flat cold-rolled stainless steel products implements the continuity and integration of the steps described below preferably starting from strips with the aforesaid features of roughness and surface cleanness.
  • the first two steps of the process contemplate the thermal annealing treatment for the re-crystallisation and crystal grain growth process so as to reach the contemplated mechanical properties, e.g. as established by the Standard EN 10088.
  • such annealing treatment by means of a predetermined and controlled oxidation, causes on the strip surface the formation of a layer of oxides and a layer of dechromized steel underneath, both layers being easily removable by means of a subsequent pickling treatment.
  • This annealing treatment is performed in at least two consecutive steps, as shown below:
  • the first heating produces an oxide suitable to limit the oxidation during the subsequent step and easily conditionable/removable during the subsequent cooling, descaling, pickling and finishing treatments.
  • the parameters controlling this first oxidation step are the content of oxygen in the annealing atmosphere, variable from 0,5 to 12%, and the heating rate of the strip whereby the average thermal flow, which the strip must receive on each face, must be comprised from 15 to 300 kW/m 2 .
  • the first heating of the strip is preferably conducted, for a strip of thickness comprised from 0,8 to 3,5 mm with an average thermal flow received by the strip, on each face, from 120 to 300 kW/m 2 and concentrations of O 2 from 0,5% and 5%, so as to favour the formation of a layer of oxide which is advantageously 30% thinner than that obtainable with the conventional procedures up to the maximum temperature contemplated for this process step.
  • the first heating step up to 650-1050°C is performed by means of an average thermal flow, received on each face of the strip, comprised in the range from 45 to 175 kW/m 2 and of concentrations of O 2 comprised from 0,5 to 5%.
  • This first heating step may occur, preferably up to 600°C, with an average thermal flow on each strip face comprised in the 150-300 kW/m 2 range.
  • This first heating may be performed by means of a first heating section provided with heating systems, e.g. constituted by burners of the conventional type and/or of the flameless type and/or of the flame impingement type, also of the self-recovery type and/or self-regenerating type, operated on natural gas and/or methane and/or LPG and using air, enriched air or pure oxygen or mixtures thereof as supporter of combustion.
  • the air is pre-heated up to a temperature of 650°C and/or enriched with oxygen up to concentrations of 31 % and/or pure oxygen.
  • Said first heating section is preferably provided with refractory materials suitable for continuous operation at temperatures also up to 1500°C.
  • the content of oxygen in the treatment atmosphere, desired for the purposes of the process, will be ensured/controlled by direct feeding systems for feeding the furnace, at controllable flow rate, with possibly enriched air or oxygen, and preferably by controlling the combustion ratio to the burner.
  • direct feeding systems may comprise lances, slots, distributors or other suitable systems.
  • the content of O 2 in the atmosphere is measured preferably at a distance from the surface of the strip comprised from 50 to 200 mm.
  • the second heating step in order to condition/limit the growth of the oxide layer, provides a control of the reactivity of the annealing gaseous atmosphere by acting on the presence of agents, such as O 2 , H 2 O and CO 2 , and preferably by operating with inert atmosphere, e.g. N 2 , whose dew temperature is comprised from -60 and 10°C or reducing atmosphere, e.g. N 2 and H 2 , whose dew temperature is from -30 to 10 °C.
  • agents such as O 2 , H 2 O and CO 2
  • Such second heating of the strip is obtained in a second dedicated heating section, fluid-dynamically separate from the first one by means of a gas seal to prevent reintroductions of external air, provided with heating systems with electrical resistors or radiating tubes.
  • the oxygen content in the atmosphere is controlled by means of appropriate feeding and exhaust systems of the gaseous chemical species belonging to the treatment atmosphere.
  • a third step of the process contemplates a cooling down to ambient temperature in which there is no further growth of the oxide layer formed during the annealing and/or the partial reduction of the iron oxides contained therein.
  • This cooling step is performed in presence of inert agents, such as N 2, and/or reducing agents H 2 .
  • the cooling step is performed preferably in atmosphere formed by mixtures of N 2 and H 2 with concentrations of H 2 comprised in the 0-50% range with a dew temperature from -60 °C and 10 °C.
  • the dew temperature is comprised from -30 °C to 10 °C.
  • the cooling down to 550°C-450°C occurs in atmosphere containing mixtures of N 2 and H 2 , with concentrations of H 2 comprised in the 0-50% range, with a dew temperature from -60°C to 10°C.
  • the cooling section is provided with systems for measuring and controlling the composition of said cooling atmosphere.
  • the cooling devices are sealed if H 2 is used.
  • the fourth step of the process contemplates at least one thermochemical descaling treatment, by means of the use of dissolved salts, or an electrolytic descaling treatment suitably performed preferably in neutral solution of Na 2 SO 4 , with concentration comprised from 130 to 210 g/I and at temperatures comprised from 40 to 90°C, or in acid solution of H 2 SO 4 , with concentration comprised from 40 to 150 g/I at temperatures comprised from 25 to 50 °C.
  • an electrolytic descaling treatments can be performed by using solutions of nitric acid with concentration between 30 and 150 g/I at temperature comprised from 30 to 70°C.
  • such descaling treatment provides a selective oxidation of the chromium present in the oxide making it soluble in the bath determining the preferably complete removal of the layer itself.
  • a preferred method for the above-mentioned descaling contemplates that the delivered electrical current and the corresponding electrical charge transferred to the strip are related to:
  • a possible application of said process contemplates the use of neutral sodium sulphate solutions with concentration equal to 160 g/l at temperature equal to 75 °C and applied current density equal to 8 A/dm 2 , and a subsequent electrolytic treatment in nitric acid at 50°C with applied current density equal to 6 A/dm 2 .
  • the fifth step of the process contemplates a possible pickling and/or passivation treatment which removes the layer of oxides, possibly residuals after the descaling treatment, and possibly the dechromized layer underneath.
  • said treatment is performed by means of the use of mineral acid solutions and HF, with HF concentration comprised from 0 to 40 g/l and preferably comprised from 0 to 15 g/l, at temperature comprised from 25 to 70 °C and preferably from 30 to 60 °C.
  • a preferred method of the present invention is the use of solutions in which the mineral acid consists of HNO 3 with concentration comprised from 40 to 200g/l and preferably comprised from 100 to 140g/l.
  • the object of the present invention further includes processes in which the mineral acid is formed by mixtures of acids selected from HNO 3 H 2 SO 4 , HCl with concentrations respectively comprised from 20-120 g/I for HNO 3 , 30-140 g/I for H 2 SO 4 , 40-180 g/I for HCl at temperatures comprised from 25 to 70°C.
  • the latter treatment is such not to produce a strong chemical etching on the surface of the strip and therefore does not affect the reflectivity and the surface features of the surface itself.
  • this treatment is preferably made using the nitric acid based pickling solutions described above but totally free from hydrofluoric acid, either free or forming a complex, with temperatures comprised from 25 to 40 °C, preferably not higher than 30°C.
  • a sealed separation chamber may be provided between the heating and cooling sections.
  • a separation chamber may be provided downstream of the cooling section to prevent the contact of potentially flammable gas with the air.
  • Said chamber may be made by means of a siphon with demineralised water or other liquids, such as for example oil, or by means of inert gas.
  • the main sections forming an annealing and pickling plant for stainless steel cold-rolled strips, in which the innovative process here described is performed for obtaining products with high surface quality tending to that currently produced with the BA process, at lower costs with respect to the BA process and minimising the environmental impact with respect to CA&PLs, are schematically shown in figure 1 .
  • numeral 1 indicates the strip heating section up to a temperature comprised in the range from 650 to 1050°C
  • numeral 2 indicates the strip heating section up to a temperature in the range from 650 to 1200°C
  • numeral 3 indicates the strip cooling section up to a temperature comprised from 650°C to the temperature in the thermochemical or electrolytic descaling section
  • numeral 5 indicates the pickling and finishing/passivation section provided with chemical baths.
  • Second heating section 2 when the use of atmospheres free from O 2 and CO 2 is contemplated, is provided with heating means, such as: radiating tubes; electrical resistors and/or inductors and/or NIR (near-infrared) heaters.
  • heating means such as: radiating tubes; electrical resistors and/or inductors and/or NIR (near-infrared) heaters.
  • Cooling section 3 consists of one or more modules using reciprocally different and maintained separate atmospheres.
  • This example describes the annealing and pickling process of an austenitic stainless steel strip of the AISI 304 type, 1 mm thick and 1270 mm wide, cold-rolled with a reduction rate of 80%, with a surface roughness (Ra) comprised from 0,08 to 0,10 ⁇ m and with an amount of residual rolling oil ⁇ 10mg/m 2 of strip, said strip having previously being subjected to degreasing in alkaline solution.
  • the strip was processed at a process speed of 130 m/min in a plant schematised in fig.1 for a production rate of approximately 78t/h. According to the present invention, operations were under the following conditions:
  • This example describes the annealing and pickling process of a ferritic stainless steel strip of the AISI 430 type, 0,7 mm thick and 1270 mm wide, cold-rolled with a reduction rate of 75% and with a surface roughness (Ra) comprised from 0,05 to 0,08 ⁇ m.
  • the strip was processed at a process speed of 130 m/min for a production rate of approximately 55 t/h. According to the present invention, the operations were under the following conditions:

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Mechanical Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
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  • Heat Treatment Of Strip Materials And Filament Materials (AREA)
  • Heat Treatment Of Sheet Steel (AREA)
  • Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
  • Manufacturing Of Steel Electrode Plates (AREA)
EP07847161A 2006-11-14 2007-11-14 Annealing and pickling process Not-in-force EP2102376B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IT002187A ITMI20062187A1 (it) 2006-11-14 2006-11-14 Processo di ricottura e decapaggio
PCT/EP2007/062319 WO2008058986A1 (en) 2006-11-14 2007-11-14 Annealing and pickling process

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EP2102376A1 EP2102376A1 (en) 2009-09-23
EP2102376B1 true EP2102376B1 (en) 2012-01-11

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EP07847161A Not-in-force EP2102376B1 (en) 2006-11-14 2007-11-14 Annealing and pickling process

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US (1) US8192566B2 (ko)
EP (1) EP2102376B1 (ko)
JP (1) JP5411704B2 (ko)
KR (1) KR101513313B1 (ko)
CN (1) CN101558173B (ko)
AT (1) ATE541061T1 (ko)
ES (1) ES2380500T3 (ko)
IT (1) ITMI20062187A1 (ko)
WO (1) WO2008058986A1 (ko)

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JP5729211B2 (ja) * 2010-08-31 2015-06-03 Jfeスチール株式会社 冷延鋼板の製造方法、冷延鋼板および自動車部材
JP5835558B2 (ja) * 2010-08-31 2015-12-24 Jfeスチール株式会社 冷延鋼板の製造方法
KR101304602B1 (ko) * 2011-12-21 2013-09-05 주식회사 포스코 스케일의 박리성을 향상시키는 방법
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KR20090089317A (ko) 2009-08-21
US20100065167A1 (en) 2010-03-18
ITMI20062187A1 (it) 2008-05-15
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CN101558173A (zh) 2009-10-14
ATE541061T1 (de) 2012-01-15
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WO2008058986A1 (en) 2008-05-22
EP2102376A1 (en) 2009-09-23

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